Treatment with topiramate in rats during childhood causes testicular structural impairment at adulthood

• Published in: Journal of developmental origins of health and disease 2023-04, Vol.14 (2), p.279-285
• Main Authors: Borges, Lorena Ireno, Forcato, Simone, do Nascimento Olanda, Lays Cristine, Frigoli, Giovanna Fachetti, Vidigal, Camila Borecki, Moura, Kawane Fabrício, Fernandes, Glaura Scantamburlo A., Franco, Maria do Carmo Pinho, Ceravolo, Graziela Scalianti, Gerardin, Daniela Cristina Ceccatto
• Format: Article
• Language: English
• Subjects: Adults; Animals; Child development; Childhood; Disease Progression; Drug dosages; Experiments; FDA approval; Hormones; Male; Male reproductive system; Motility; Original Article; Ostomy; PCB; Physiology; Polychlorinated biphenyls; Puberty; Rats; Semen; Sperm; Spermatozoa; Systems development; Teenagers; Testis; Testosterone; Topiramate
• ISSN: 2040-1744; 2040-1752
• DOI: 10.1017/S2040174422000587

Topiramate (TOP) is a psychotropic drug prescribed for the treatment of epilepsy in children older than 2 years of age and for migraine prophylaxis in adolescents. There is evidence that TOP promotes negative effects on the reproductive system of male rats. This study aimed to evaluate the immediate and late treatment effects of TOP during childhood and adolescence on the male rat reproductive system. Two experimental groups received 41 mg/kg of TOP daily, by gavage, from postnatal day (PND) 16 to 28 (TOPc group) or from PND 28 to 50 (TOPa group). Control groups (CTRc group or CTRa group) received water daily. Half of the anim–als were evaluated 24 h after the end of treatment (PND 29 and PND 51, respectively) and the remainder were evaluated in adulthood (PND120). The following parameters were determined: anogenital distance, sperm evaluation, testis’ histomorphometry and plasma testosterone concentration. At PND 120, the volume (CTRc:62.58 ± 2.13; TOPc: 54.54 ± 2.10*%, p = 0.018) and total length (CTRc: 25.48 ± 1.61; TOPc: 18.94 ± 2.41*, p = 0.035) of seminiferous tubules were decreased and the volume of interstitial tissue (CTRc:37.41 ± 2.13; TOPc: 45.45 ± 2.09*%, p = 0.018) and number of Leydig cells/testis (CTRc: 277.00 ± 36.70; TOPc: 400.20 ± 13.23*, p = 0.013) were increased in the TOPc group. The other parameters remained similar between the groups. Therefore, the present study contributes to our understanding that childhood treatment with TOP has an impact on the rat reproductive system in adulthood, suggesting that this period is more sensitive to TOP exposure than adolescence.